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5-氨基酮戊酸-透明质酸复合物增强 5-氨基酮戊酸在皮肤中的滞留及其治疗增生性瘢痕的疗效

5-Aminolevulinic Acid-Hyaluronic Acid Complexes Enhance Skin Retention of 5-Aminolevulinic Acid and Therapeutic Efficacy in the Treatment of Hypertrophic Scar.

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, University Town, Guangzhou, 510006, People's Republic of China.

出版信息

AAPS PharmSciTech. 2022 Aug 5;23(6):216. doi: 10.1208/s12249-022-02370-1.

DOI:10.1208/s12249-022-02370-1
PMID:35927520
Abstract

Hypertrophic scar is a serious skin disorder, which reduces the patient's quality of life. 5-aminolevulinic acid (5-ALA)-mediated photodynamic therapy has been used to treat patients with hypertrophic scar. However, the poor skin retention of 5-ALA limited the therapeutic effect. In this study, we constructed the 5-ALA-hyaluronic acid (HA) complex to potentially prolong the skin retention of 5-ALA for improving the therapeutic efficacy. HA is a polysaccharide with viscoelasticity and the carboxyl groups could conjugate with amino groups of 5-ALA via electrostatic interaction. The protoporphyrin IX (PpIX) assay revealed that 5-ALA-HA complexes markedly enhanced the skin retention, resulting in increased generation and accumulation of endogenous photosensitizer PpIX. Furthermore, 5-ALA-HA complexes allowed PpIX to be maintained at a high level for 12 h, much longer than the 3 h of 5-ALA alone. And then, the accumulative PpIX induced by 5-ALA-HA in human hypertrophic scar fibroblasts (HSF) was triggered by laser irradiation to produce sufficient reactive oxygen species, leading to efficient necrosis and apoptosis of HSF. In vivo therapeutic efficacy study indicated that 5-ALA-HA effectively reduced the appearance and scar thickness, and the scar elevation index with 5-ALA-HA treatment was significantly lower than other groups, suggesting that the 5-ALA-HA-treated scar became flattened and was closely matched to the unwounded tissues. Moreover, 5-ALA-HA treatment markedly downregulated the gene expression levels of α-SMA and TGF-β1, demonstrating attenuated the scar formation and growth. Therefore, the 5-ALA-HA complex enhancing skin retention and PpIX accumulation at the lesion site provide a promising therapeutic strategy for hypertrophic scar.

摘要

增生性瘢痕是一种严重的皮肤疾病,会降低患者的生活质量。5-氨基酮戊酸(5-ALA)介导的光动力疗法已被用于治疗增生性瘢痕患者。然而,5-ALA 的皮肤滞留率低限制了其治疗效果。在本研究中,我们构建了 5-ALA-透明质酸(HA)复合物,以期延长 5-ALA 在皮肤中的滞留时间,从而提高治疗效果。HA 是一种具有粘弹性的多糖,其羧基可通过静电相互作用与 5-ALA 的氨基结合。原卟啉 IX(PpIX)测定显示,5-ALA-HA 复合物显著增强了皮肤的滞留性,导致内源性光敏剂 PpIX 的生成和积累增加。此外,5-ALA-HA 复合物使 PpIX 能够保持在高水平长达 12 小时,比单独使用 5-ALA 的 3 小时长得多。然后,激光照射可引发由 5-ALA-HA 在人增生性瘢痕成纤维细胞(HSF)中累积的 PpIX 产生足够的活性氧,导致 HSF 的有效坏死和凋亡。体内治疗效果研究表明,5-ALA-HA 可有效减少外观和瘢痕厚度,且 5-ALA-HA 治疗的瘢痕隆起指数明显低于其他组,表明经 5-ALA-HA 治疗的瘢痕变平并与未受伤组织紧密匹配。此外,5-ALA-HA 治疗显著下调了 α-SMA 和 TGF-β1 的基因表达水平,表明瘢痕形成和生长受到抑制。因此,5-ALA-HA 复合物可增强病变部位的皮肤滞留和 PpIX 积累,为增生性瘢痕提供了一种有前途的治疗策略。

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